Erythrocyte Binding Activity Displayed by a Selective Group of Plasmodium vivax Tryptophan Rich Antigens Is Inhibited by Patients' Antibodies

被引:24
|
作者
Tyagi, Rupesh Kumar [1 ]
Sharma, Yagya Dutta [1 ]
机构
[1] All India Inst Med Sci, Dept Biotechnol, New Delhi 110029, India
来源
PLOS ONE | 2012年 / 7卷 / 12期
关键词
RESISTANCE-ASSOCIATED MUTATIONS; DIHYDROPTEROATE SYNTHASE; IMMUNOLOGICAL RESPONSES; DIHYDROFOLATE-REDUCTASE; MALARIA; FALCIPARUM; PROTEIN; IDENTIFICATION; INVASION; EXPRESSION;
D O I
10.1371/journal.pone.0050754
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plasmodium vivax is a very common but non-cultivable malaria parasite affecting large human population in tropical world. To develop therapeutic reagents for this malaria, the parasite molecules involved in host-parasite interaction need to be investigated as they form effective vaccine or drug targets. We have investigated here the erythrocyte binding activity of a group of 15 different Plasmodium vivax tryptophan rich antigens (PvTRAgs). Only six of them, named PvTRAg, PvTRAg38, PvTRAg33.5, PvTRAg35.2 PvTRAg69.4 and PvATRAg74, showed binding to host erythrocytes. That the PvTRAgs binding to host erythrocytes was specific was evident from the competitive inhibition and saturation kinetics results. The erythrocyte receptors for these six PvTRAgs were resistant to trypsin and neuraminidase. These receptors were also chymotrypsin resistant except the receptors for PvTRAg38 and PvATRAg74 which were partially sensitive to this enzyme. The cross-competition studies showed that the chymotrypsin resistant RBC receptor for each of these two proteins was different. Altogether, there seems to be three RBC receptors for these six PvTRAgs and each PvTRAg has two RBC receptors. Both RBC receptors for PvTRAg, PvTRAg69.4, PvTRAg33.5, and PvTRAg35.2 were common to all these four proteins. These four PvTRAgs also shared one of their RBC receptors with PvTRAg38 as well as with PvATRAg74. The erythrocyte binding activity of these six PvTRAgs was inhibited by the respective rabbit polyclonal antibodies as well as by the natural antibodies produced by the P. vivax exposed individuals. It is concluded that only selective few PvTRAgs show erythrocyte binding activity involving different receptor molecules which can be blocked by the natural antibodies. Further studies on these receptor and ligands may lead to the development of therapeutic reagents for P. vivax malaria. Citation: Tyagi RK, Sharma YD (2012) Erythrocyte Binding Activity Displayed by a Selective Group of Plasmodium vivax Tryptophan Rich Antigens Is Inhibited by Patients' Antibodies. PLoS ONE 7(12): e50754. doi:10.1371/journal.pone.0050754
引用
收藏
页数:14
相关论文
共 32 条
  • [1] Erythrocyte binding activity of Plasmodium vivax tryptophan rich antigens is inhibited by patients’ antibodies
    Rupesh K Tyagi
    Yagya D Sharma
    [J]. Malaria Journal, 11 (Suppl 1)
  • [2] Defining the Erythrocyte Binding Domains of Plasmodium vivax Tryptophan Rich Antigen 33.5
    Bora, Hema
    Tyagi, Rupesh Kumar
    Sharma, Yagya Dutta
    [J]. PLOS ONE, 2013, 8 (04):
  • [3] Receptor specific binding regions of Plasmodium vivax tryptophan rich antigens and parasite growth inhibition activity of PvTRAg35.2
    Alam, Mohd Shoeb
    Zeeshan, Mohammad
    Mittra, Pooja
    Choudhary, Vandana
    Sharma, Yagya D.
    [J]. MICROBES AND INFECTION, 2016, 18 (09) : 550 - 558
  • [4] High immunogenecity and erythrocyte-binding activity in the tryptophan-rich domain (TRD) of the 74-kDa Plasmodium vivax alanine-tryptophan-rich antigen (PvATRAg74)
    Alam, Mohammad Tauqeer
    Bora, Hema
    Singh, Neeru
    Sharma, Yagya D.
    [J]. VACCINE, 2008, 26 (31) : 3787 - 3794
  • [5] Presence of Memory T Cells and Naturally Acquired Antibodies in Plasmodium vivax Malaria-Exposed Individuals Against a Group of Tryptophan-Rich Antigens With Conserved Sequences
    Zeeshan, Mohammad
    Bora, Hema
    Sharma, Yagya Dutta
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2013, 207 (01): : 175 - 185
  • [6] CD4+ T Cell Response Correlates with Naturally Acquired Antibodies against Plasmodium vivax Tryptophan-Rich Antigens
    Zeeshan, Mohammad
    Tyagi, Kriti
    Sharma, Yagya D.
    [J]. INFECTION AND IMMUNITY, 2015, 83 (05) : 2018 - 2029
  • [7] Evidence for diversifying selection on erythrocyte-binding antigens of Plasmodium falciparum and P-vivax
    Baum, J
    Thomas, AW
    Conway, DJ
    [J]. GENETICS, 2003, 163 (04) : 1327 - 1336
  • [8] Plasmodium vivax invasion of human erythrocytes inhibited by antibodies directed against the Duffy binding protein
    Grimberg, Brian T.
    Udomsangpetch, Rachanee
    Xainli, Jia
    McHenry, Amy
    Panichakul, Tasanee
    Sattabongkot, Jetsumon
    Cui, Liwang
    Bockarie, Moses
    Chitnis, Chetan
    Adams, John
    Zimmerman, Peter A.
    King, Christopher L.
    [J]. PLOS MEDICINE, 2007, 4 (12): : 1940 - 1948
  • [9] Plasmodium vivax immunological properties of tryptophan-rich antigens PvTRAg 35 2 and PvTRAg 80 6
    Mittra, Pooja
    Singh, Neeru
    Sharma, Yagya D.
    [J]. MICROBES AND INFECTION, 2010, 12 (12-13) : 1019 - 1026
  • [10] Recognition of Human Erythrocyte Receptors by the Tryptophan-Rich Antigens of Monkey Malaria Parasite Plasmodium knowlesi
    Tyagi, Kriti
    Gupta, Deepali
    Saini, Ekta
    Choudhary, Shilpa
    Jamwal, Abhishek
    Alam, Mohd. Shoeb
    Zeeshan, Mohammad
    Tyagi, Rupesh K.
    Sharma, Yagya D.
    [J]. PLOS ONE, 2015, 10 (09):